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Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma

BACKGROUND: Several recent studies demonstrated that microRNAs (miRNAs) are stably detectable in plasma/serum. We hypothesised that plasma miRNAs concentrations contributed to potential biomarkers in patients with oesophageal squamous cell carcinoma (ESCC). METHODS: We selected three oncogenic miRNA...

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Autores principales: Komatsu, S, Ichikawa, D, Takeshita, H, Tsujiura, M, Morimura, R, Nagata, H, Kosuga, T, Iitaka, D, Konishi, H, Shiozaki, A, Fujiwara, H, Okamoto, K, Otsuji, E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137413/
https://www.ncbi.nlm.nih.gov/pubmed/21673684
http://dx.doi.org/10.1038/bjc.2011.198
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author Komatsu, S
Ichikawa, D
Takeshita, H
Tsujiura, M
Morimura, R
Nagata, H
Kosuga, T
Iitaka, D
Konishi, H
Shiozaki, A
Fujiwara, H
Okamoto, K
Otsuji, E
author_facet Komatsu, S
Ichikawa, D
Takeshita, H
Tsujiura, M
Morimura, R
Nagata, H
Kosuga, T
Iitaka, D
Konishi, H
Shiozaki, A
Fujiwara, H
Okamoto, K
Otsuji, E
author_sort Komatsu, S
collection PubMed
description BACKGROUND: Several recent studies demonstrated that microRNAs (miRNAs) are stably detectable in plasma/serum. We hypothesised that plasma miRNAs concentrations contributed to potential biomarkers in patients with oesophageal squamous cell carcinoma (ESCC). METHODS: We selected three oncogenic miRNAs (miR-21, miR-184, miR-221) and one tumour suppressive miRNA (miR-375), which are frequently reported in squamous cell carcinoma, as candidate targets for this plasma miRNA assay. This study was divided into three steps: (1) Determination of appropriate plasma miRNAs in preliminary tests. (2) Evaluation of whether the plasma miRNA assays could monitor tumour dynamics. (3) Validation study on the clinical application of plasma miRNA assays in 50 ESCC patients and 20 healthy volunteers. RESULTS: (1) In preliminary tests, the plasma level of miR-21 was significantly higher (P=0.0218) and that of miR-375 (P=0.0052) was significantly lower in ESCC patients than controls. (2) The high plasma miR-21 levels reflected tumour levels in all cases (100%). The plasma level of miR-21 was significantly reduced in postoperative samples (P=0.0058). (3) On validation analysis, the plasma level of miR-21 tended to be higher in ESCC patients (P=0.0649), while that of miR-375 was significantly lower (P<0.0001) and the miR-21/miR-375 ratio was significantly higher (P<0.0001) in ESCC patients than in controls. The value of the area under the receiver-operating characteristic curve (AUC) was 0.816 for the miR-21/miR-375 ratio assay. Patients with a high plasma level of miR-21 tended to have greater vascular invasion (P=0.1554) and to show a high correlation with recurrence (P=0.0164). CONCLUSION: Detection of circulating miRNAs might provide new complementary tumour markers for ESCC.
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spelling pubmed-31374132012-06-28 Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma Komatsu, S Ichikawa, D Takeshita, H Tsujiura, M Morimura, R Nagata, H Kosuga, T Iitaka, D Konishi, H Shiozaki, A Fujiwara, H Okamoto, K Otsuji, E Br J Cancer Molecular Diagnostics BACKGROUND: Several recent studies demonstrated that microRNAs (miRNAs) are stably detectable in plasma/serum. We hypothesised that plasma miRNAs concentrations contributed to potential biomarkers in patients with oesophageal squamous cell carcinoma (ESCC). METHODS: We selected three oncogenic miRNAs (miR-21, miR-184, miR-221) and one tumour suppressive miRNA (miR-375), which are frequently reported in squamous cell carcinoma, as candidate targets for this plasma miRNA assay. This study was divided into three steps: (1) Determination of appropriate plasma miRNAs in preliminary tests. (2) Evaluation of whether the plasma miRNA assays could monitor tumour dynamics. (3) Validation study on the clinical application of plasma miRNA assays in 50 ESCC patients and 20 healthy volunteers. RESULTS: (1) In preliminary tests, the plasma level of miR-21 was significantly higher (P=0.0218) and that of miR-375 (P=0.0052) was significantly lower in ESCC patients than controls. (2) The high plasma miR-21 levels reflected tumour levels in all cases (100%). The plasma level of miR-21 was significantly reduced in postoperative samples (P=0.0058). (3) On validation analysis, the plasma level of miR-21 tended to be higher in ESCC patients (P=0.0649), while that of miR-375 was significantly lower (P<0.0001) and the miR-21/miR-375 ratio was significantly higher (P<0.0001) in ESCC patients than in controls. The value of the area under the receiver-operating characteristic curve (AUC) was 0.816 for the miR-21/miR-375 ratio assay. Patients with a high plasma level of miR-21 tended to have greater vascular invasion (P=0.1554) and to show a high correlation with recurrence (P=0.0164). CONCLUSION: Detection of circulating miRNAs might provide new complementary tumour markers for ESCC. Nature Publishing Group 2011-06-28 2011-06-14 /pmc/articles/PMC3137413/ /pubmed/21673684 http://dx.doi.org/10.1038/bjc.2011.198 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Molecular Diagnostics
Komatsu, S
Ichikawa, D
Takeshita, H
Tsujiura, M
Morimura, R
Nagata, H
Kosuga, T
Iitaka, D
Konishi, H
Shiozaki, A
Fujiwara, H
Okamoto, K
Otsuji, E
Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma
title Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma
title_full Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma
title_fullStr Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma
title_full_unstemmed Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma
title_short Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma
title_sort circulating micrornas in plasma of patients with oesophageal squamous cell carcinoma
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3137413/
https://www.ncbi.nlm.nih.gov/pubmed/21673684
http://dx.doi.org/10.1038/bjc.2011.198
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